MeSH Treeview
Query OMIM entry list
162350
CLN4B
CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Glioma
Astrocytoma
Neoplasms, Glandular and Epithelial
Neoplasms, Neuroepithelial
Glioma
Astrocytoma
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neoplasms, Neuroepithelial
Glioma
Astrocytoma
Neoplasms by Site
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Brain Neoplasms
Dementia
Epilepsy
Epilepsies, Myoclonic
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Seizures
Movement Disorders
Parkinsonian Disorders
Nervous System Neoplasms
Central Nervous System Neoplasms
Brain Neoplasms
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Neuronal Ceroid-Lipofuscinoses
Neurologic Manifestations
Dyskinesias
Myoclonus
Seizures
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Neuronal Ceroid-Lipofuscinoses
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Lipidoses
Neuronal Ceroid-Lipofuscinoses
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Lipidoses
Neuronal Ceroid-Lipofuscinoses
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Lipidoses
Neuronal Ceroid-Lipofuscinoses
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Myoclonus
Seizures
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